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What works? What matters? ClinPage's series of audio interviews explores the practicalities of pivotal technologies and services in global research. If your organization has a thought leader with something to say, please contact .(JavaScript must be enabled to view this email address) To hear about podcast sponsorship opportunities, .(JavaScript must be enabled to view this email address)
Guest: Michael Ibara, Pfizer

Between A Rock And The FDA

April 22, 2010
LENGTH: 40:01

Michael Ibara, head of pharmacovigilance information management at Pfizer, discusses the intricacies of how to manage drug safety data in an increasingly electronic age. But the context of his remarks is much larger, and involves how both industry and government may be able to convince the public that all reasonable measures are being made to keep medicines as safe as possible. 

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Guest: Roy Vagelos, Merck

Merck’s Finest Hour

May 29, 2009
LENGTH: 14:00

Roy Vagelos may be retired, but he remains a legend all the same. The former Merck leader spoke at this year’s Clinical Trials Congress.

His remarks covered a lot of ground. In a 14-minute podcast, we include two key sections of his presentation.

The first concerns the company’s development of a cure (yes, that’s the right word) for river blindness in sub-Saharan Africa. 

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Guest: Landen Bain, CDISC

Eclinical, Health Record Integration

February 25, 2009
LENGTH: 14:00

In 2009, it is easier and more feasible to connect two vast data cosmos that have long existed separately. The electronic data capture (EDC) systems for clinical research are slowly being connected to larger, more general-purpose electronic health record (EHR) systems for physicians. 

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December 13, 2017

Guest: Paul Clarkson, Genentech

Podcast: Making Smart Protocols

As a trustee of the Society for Clinical Data Management (SCDM), Paul Clarkson is the archetype of the data manager who understands the largest issues affecting clinical development. As director of data management at Genentech, he’s been thinking about how data managers can help their organizations develop better protocols. 

Guest: Anthony Costello

Clinical Data in 2017

The burden of day-to-day responsibilities does not always allow for appropriate reflection on the future. The Society for Clinical Data Management is trying to address that next month in its annual Leadership Forum. 

Guest: Carol Rozwell

The Case For Standards Now

Gartner’s Carol Rozwell is one of the industry’s leading authorities on technology adoption and clinical data standards. In this illuminating interview with ClinPage editor Mark Uehling, she discusses why some organizations hesitate to use CDISC standards and how some contract research organizations (CRO) have recently begun to see data standards differently. 


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